spreading the word

17 Feb

For all of you CF families out there, there is a fantastic new website called CysticLife. It works kinds of like Facebook, networking families and individuals with CF. It is a great community to go to for help, encouragement and general info. Check it out! You’ll love it!

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4 Responses to “spreading the word”

  1. Anonymous February 18, 2010 at 4:24 am #

    Now that CF seems to be coming up more and more, I look for sites that have information and discussion boards. My sister passed away it will be 10 years ago this coming October and I miss her so much. Reading peoples stories just brings her back home, because some of what I hear are her exact words. Let't keep up the good and infromative site.Thank You.

  2. Anonymous February 18, 2010 at 10:15 am #

    I coach (soccer) a young boy, Nat Gallen, who is fighting CF. I used to be a professional soccer player and now do some pretty cool things in the "self-help" world. I decided to make a movie to help raise funds for the Cystic Fibrosis Foundation. The result is FIGHT-The Movie. It's a 2 hour inspirational movie sharing the stories of 11 everyday people who choose to FIGHT. My definition of FIGHT is:fight [fayht] v. To exert oneself continuously and vigorously toward a desired outcome; to steadily progress in the direction of a dream.***For more information or to order a copy of FIGHT-The Movie, visit:www.iamreadytofight.comTO A CURE!Jerry Moyerjerry@iamreadytofight.com

  3. Lisa P February 18, 2010 at 12:23 pm #

    Anonymous #1: I'm so sorry to hear about your sister. I'm glad that participating in CF communities and forums brings up fond memories of her.

  4. Lisa P February 18, 2010 at 12:23 pm #

    Jerry: I'll be sure to check out your site!

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